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SNORD14D (small nucleolar RNA, C/D box 14D)

Identity

Other alias-
HGNC (Hugo) SNORD14D
LocusID (NCBI) 85390
Atlas_Id 79538
Location 11q24.1  [Link to chromosome band 11q24]
Location_base_pair Starts at 123058909 and ends at 123058995 bp from pter ( according to hg38-Dec_2013)

Note

Non-annotated gene. Preliminary data : if you are an author
who wish to write a full paper/card on this gene, go to  How to contribute

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)SNORD14D   30353
Cards
Entrez_Gene (NCBI)SNORD14D  85390  small nucleolar RNA, C/D box 14D
Aliases
GeneCards (Weizmann)SNORD14D
Ensembl hg19 (Hinxton)ENSG00000207118 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000207118 [Gene_View]  chr11:123058909-123058995 [Contig_View]  SNORD14D [Vega]
ICGC DataPortalENSG00000207118
TCGA cBioPortalSNORD14D
AceView (NCBI)SNORD14D
Genatlas (Paris)SNORD14D
WikiGenes85390
SOURCE (Princeton)SNORD14D
Genetics Home Reference (NIH)SNORD14D
Genomic and cartography
GoldenPath hg38 (UCSC)SNORD14D  -     chr11:123058909-123058995 -  11q24.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SNORD14D  -     11q24.1   [Description]    (hg19-Feb_2009)
EnsemblSNORD14D - 11q24.1 [CytoView hg19]  SNORD14D - 11q24.1 [CytoView hg38]
Mapping of homologs : NCBISNORD14D [Mapview hg19]  SNORD14D [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)SNORD14D
Alternative Splicing GalleryENSG00000207118
Gene ExpressionSNORD14D [ NCBI-GEO ]   SNORD14D [ EBI - ARRAY_EXPRESS ]   SNORD14D [ SEEK ]   SNORD14D [ MEM ]
Gene Expression Viewer (FireBrowse)SNORD14D [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)85390
GTEX Portal (Tissue expression)SNORD14D
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORD14D
DMDM Disease mutations85390
Blocks (Seattle)SNORD14D
Human Protein AtlasENSG00000207118
Protein Interaction databases
FunCoupENSG00000207118
BioGRIDSNORD14D
STRING (EMBL)SNORD14D
ZODIACSNORD14D
Ontologies - Pathways
Huge Navigator SNORD14D [HugePedia]
snp3D : Map Gene to Disease85390
BioCentury BCIQSNORD14D
ClinGenSNORD14D
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD85390
Chemical/Pharm GKB GenePA165543685
Clinical trialSNORD14D
Miscellaneous
canSAR (ICR)SNORD14D (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORD14D
EVEXSNORD14D
GoPubMedSNORD14D
iHOPSNORD14D
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Sep 18 13:39:37 CEST 2017

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